Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Abigail Crisp-Hihn"'
Autor:
Jonas Carlsson Almlöf, Per Lundmark, Anders Lundmark, Bing Ge, Seraya Maouche, Harald H H Göring, Ulrika Liljedahl, Camilla Enström, Jessy Brocheton, Carole Proust, Tiphaine Godefroy, Jennifer G Sambrook, Jennifer Jolley, Abigail Crisp-Hihn, Nicola Foad, Heather Lloyd-Jones, Jonathan Stephens, Rhian Gwilliam, Catherine M Rice, Christian Hengstenberg, Nilesh J Samani, Jeanette Erdmann, Heribert Schunkert, Tomi Pastinen, Panos Deloukas, Alison H Goodall, Willem H Ouwehand, François Cambien, Ann-Christine Syvänen
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e52260 (2012)
A large number of genome-wide association studies have been performed during the past five years to identify associations between SNPs and human complex diseases and traits. The assignment of a functional role for the identified disease-associated SN
Externí odkaz:
https://doaj.org/article/d0a286581c23430fa9c2b3d1ada6f11f
Autor:
Mike Clark, Kottekkattu Balan, Louise Hawkins, Amanda C. Evans, Kathryn L. Armour, Nicola Grehan, Lorna M. Williamson, Stephen F. Garner, Cedric Ghevaert, Paul Lloyd-Evans, Nina Herbert, Abigail Crisp-Hihn, Philip Cookson, Willem H. Ouwehand
Publikováno v:
Blood. 122:313-320
Fetomaternal alloimmune thrombocytopenia, caused by the maternal generation of antibodies against fetal human platelet antigen-1a (HPA-1a), can result in intracranial hemorrhage and intrauterine death. We have developed a therapeutic human recombinan
Autor:
Per Lundmark, Abigail Crisp-Hihn, Seraya Maouche, Tiphaine Godefroy, Harald H H Göring, Nilesh J. Samani, Anders Lundmark, Carole Proust, Jonathan Stephens, François Cambien, Jessy Brocheton, Bing Ge, Nicola S. Foad, Heribert Schunkert, Ulrika Liljedahl, Tomi Pastinen, Panos Deloukas, Camilla Enström, Jennifer Jolley, Rhian Gwilliam, Heather Lloyd-Jones, Ann-Christine Syvänen, Alison H. Goodall, Jonas Carlsson Almlöf, Jeanette Erdmann, Willem H. Ouwehand, Jennifer G. Sambrook, Catherine M. Rice, Christian Hengstenberg
Publikováno v:
PLoS ONE; Vol 7
PLoS ONE
PLoS ONE, Vol 7, Iss 12, p e52260 (2012)
PLoS ONE
PLoS ONE, Vol 7, Iss 12, p e52260 (2012)
A large number of genome-wide association studies have been performed during the past five years to identify associations between SNPs and human complex diseases and traits. The assignment of a functional role for the identified disease-associated SN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c26502286334aa82a5f081f2917b2ea
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-195164
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-195164